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ANTIOXIDANT RESPONSE IN BRAIN TISSUSE OF CAPOETA UMBLA EXPOSED TO CHLORPYRIFOS

Yıl 2024, Cilt: 11 Sayı: 4, 1149 - 1153, 12.10.2024
https://doi.org/10.30910/turkjans.1546985

Öz

In this study on the toxic effects of chlorpyrifos on aquatic ecosystems, Capoeta umbla fish were used as a model organism. By applying chlorpyrifos to fish at different concentrations (55-110 µg/L) and durations (24 and 96 hours), malondialdehyde (MDA) levels, an indicator of lipid peroxidation in brain tissue, and catalase (CAT) and glutathione reductase (GR) activities, which are important enzymes of the antioxidant defense system, were determined. The results obtained showed that chlorpyrifos triggered oxidative stress in fish, increased lipid peroxidation in cell membranes, and suppressed the antioxidant defense system. This situation emphasizes the negative effects of chlorpyrifos on living organisms in aquatic ecosystems and its environmental risk.

Kaynakça

  • Ahmad, I., Hamid, T., Fatima, M., Chand, H. S., Jain, S. K., Athar, M., Raisuddin, S. 2000. Induction of hepatic antioxidants in freshwater catfish (Channa punctatus Bloch) is a biomarker of paper mill effluent exposure. Biochimica et Biophysica Acta (BBA)-General Subjects, 1523(1): 37-48.
  • Almeida, M., Fanini, F., Davino, S., Aznar, A., Koch, O., Barros, S. d. M. 1997. Pro-and anti-oxidant parameters in rat liver after short term exposure to hexachlorobenzene. Human & experimental toxicology, 16(5): 257-261.
  • Alves, S. R., Severino, P. c. C., Ibbotson, D. P., da Silva, A. Z., Lopes, F. R., Sáenz, L. A., Bainy, A. C. 2002. Effects of furadan in the brown mussel Perna perna and in the mangrove oyster Crassostrea rhizophorae. Marine Environmental Research, 54(3-5): 241-245.
  • Avci, A., Kaçmaz, M., Durak, İ. 2005. Peroxidation in muscle and liver tissues from fish in a contaminated river due to a petroleum refinery industry. Ecotoxicology and Environmental Safety, 60(1): 101-105.
  • Begum, G., Vijayaraghan, S. 1996. Alterations in protein metabolism of muscle tissue in the fish Clarias batrachus (Linn) by commercial grade dimethoate.
  • Beutler, E. 1984. A manual of biochemical methods. Red cell metabolism: 77-78.
  • Dar, O. I., Aslam, R., Pan, D., Sharma, S., Andotra, M., Kaur, A., Jia, A.-Q., Faggio, C. 2022. Source, bioaccumulation, degradability and toxicity of triclosan in aquatic environments: A review. Environmental Technology & Innovation, 25: 102122.
  • Hai, D. Q., Varga, S. I., Matkovics, B. 1997. Organophosphate effects on antioxidant system of carp (Cyprinus carpio) and catfish (Ictalurus nebulosus). Comparative Biochemistry and Physiology - C Pharmacology Toxicology and Endocrinology, 117(1): 83-88.
  • Hatami, M., Banaee, M., Haghi, B. N. 2019. Sub-lethal toxicity of chlorpyrifos alone and in combination with polyethylene glycol to common carp (Cyprinus carpio). Chemosphere, 219: 981-988.
  • Jin, Y., Chen, R., Liu, W., Fu, Z. 2010. Effect of endocrine disrupting chemicals on the transcription of genes related to the innate immune system in the early developmental stage of zebrafish (Danio rerio). Fish & Shellfish Immunology, 28(5-6): 854-861.
  • Jin, Y., Zhang, X., Shu, L., Chen, L., Sun, L., Qian, H., Liu, W., Fu, Z. 2010. Oxidative stress response and gene expression with atrazine exposure in adult female zebrafish (Danio rerio). Chemosphere, 78(7): 846-852.
  • Kavitha, P., Rao, J. V. 2007. Oxidative stress and locomotor behaviour response as biomarkers for assessing recovery status of mosquito fish, Gambusia affinis after lethal effect of an organophosphate pesticide, monocrotophos. Pesticide biochemistry and physiology, 87(2): 182-188.
  • Kelly, K., Havrilla, C. M., Brady, T. C., Abramo, K. H., Levin, E. D. 1998. Oxidative stress in toxicology: established mammalian and emerging piscine model systems. Environmental health perspectives, 106(7): 375-384.
  • Kirici, M. 2021. Toxicological Effects of Metal Ions and Some Pesticides on Carbonic Anhydrase Activity Purified from Bighead Carp (Hypophthalmichthys Nobilis) Gill Tissue. Carpathian Journal of Earth and Environmental Sciences, 16(1): 59-65.
  • Kirici, M., Atamanalp, M., Kirici, M., Beydemir, S. 2017. In vitro effects of some metal ions on glutathione reductase in the gills and liver of Capoeta trutta. Regulatory Mechanisms in Biosystems, 8(1): 66-70.
  • Kırıcı, M., Atamanalp, M., Kırıcı, M., Beydemir, Ş. 2020. Purification of glucose 6-phosphate dehydrogenase from Capoeta umbla gill and liver tissues and inhibition effects of some metal ions on enzyme activity. Marine Science and Technology Bulletin, 9(2): 92-101.
  • Kirici, M., Demir, Y., Beydemir, S., Atamanalp, M. 2016. The Effect of Al(3+) and Hg(2+) on Glucose 6-Phosphate Dehydrogenase from Capoeta Umbla Kidney. Applied Ecology and Environmental Research, 14(2): 253-264.
  • Kırıcı, M., Kırıcı, M., Atamanalp, M. 2017. In vitro Inhibition Effects of Some Metal Ions on Glutathione Reductase Purified from Capoeta trutta Kidney. Aquaculture Studies, 17: 385-394.
  • Kırıcı, M., Kırıcı, M., Atamanalp, M., Beydemir, Ş. 2021. Purification of glutathione reductase from some tissues of Capoeta umbla and the inhibitory effects of some metal ions on enzyme activity. Marine Science and Technology Bulletin, 10(2): 193-200.
  • Kirici, M., Kirici, M., Beydemir, S., Atamanalp, M. 2016. Purification of Carbonic Anhydrase from Capoeta umbla (Heckel, 1843) Gills and Toxicological Effects of Some Metals on Enzyme Activity. Turkish Journal of Fisheries and Aquatic Sciences, 16(1): 169-175.
  • Kirici, M., Kirici, M., Beydemir, S., Bulbul, M. 2017. Purification of Glucose 6-Phosphate Dehydrogenase from Gilthead Sea Bream (Sparus Aurata) Gill and Liver Tissues and Inhibition Effects of Some Metal Ions on Enzyme Activity. Fresenius Environmental Bulletin, 26(12): 7074-7082.
  • Kirici, M., Nedzvetsky, V. S., Agca, C. A., Gasso, V. Y. 2019. Sublethal doses of copper sulphate initiate deregulation of glial cytoskeleton, NF-kappa B and PARP expression in Capoeta umbla brain tissue. Regulatory Mechanisms in Biosystems, 10(1): 103-110.
  • Li, F., Ji, L., Luo, Y., Oh, K. 2007. Hydroxyl radical generation and oxidative stress in Carassius auratus liver as affected by 2, 4, 6-trichlorophenol. Chemosphere, 67(1): 13-19.
  • Liu, Y., Wang, J., Wei, Y., Zhang, H., Xu, M., Dai, J. 2008. Induction of time-dependent oxidative stress and related transcriptional effects of perfluorododecanoic acid in zebrafish liver. Aquatic Toxicology, 89(4): 242-250.
  • Lowry, O. H., Rosebrough, N. J., Farr, A. L., Randall, R. J. 1951. Protein measurement with the Folin phenol reagent. Journal of Biological Chemistry, 193(1): 265-275.
  • Lu, J., Wu, L., Newman, J., Faber, B., Gan, J. 2006. Degradation of pesticides in nursery recycling pond waters. Journal of agricultural and food chemistry, 54(7): 2658-2663.
  • Monteiro, P., Reis-Henriques, M., Coimbra, J. 2000. Plasma steroid levels in female flounder (Platichthys flesus) after chronic dietary exposure to single polycyclic aromatic hydrocarbons. Marine Environmental Research, 49(5): 453-467.
  • Ohkawa, H., Ohishi, N., Yagi, K. 1979. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Analytical Biochemistry, 95(2): 351-358.
  • Oruc, E. O., Sevgiler, Y., Uner, N. 2004. Tissue-specific oxidative stress responses in fish exposed to 2, 4-D and azinphosmethyl. Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology, 137(1): 43-51.
  • Oruç, E. Ö. 2010. Oxidative stress, steroid hormone concentrations and acetylcholinesterase activity in Oreochromis niloticus exposed to chlorpyrifos. Pesticide biochemistry and physiology, 96(3): 160-166.
  • Saha, S., Chukwuka, A. V., Mukherjee, D., Patnaik, L., Nayak, S., Dhara, K., Saha, N. C., Faggio, C. 2021. Chronic effects of Diazinon® exposures using integrated biomarker responses in freshwater walking catfish, Clarias batrachus. Applied Sciences, 11(22): 10902.
  • Sayeed, I., Parvez, S., Pandey, S., Bin-Hafeez, B., Haque, R., Raisuddin, S. 2003. Oxidative stress biomarkers of exposure to deltamethrin in freshwater fish, Channa punctatus Bloch. Ecotoxicology and Environmental Safety, 56(2): 295-301.
  • Sharma, S., Dar, O. I., Singh, K., Kaur, A., Faggio, C. 2021. Triclosan elicited biochemical and transcriptomic alterations in Labeo rohita larvae. Environmental Toxicology and Pharmacology, 88: 103748.
  • Thomas, P., Murthy, T. 1976. Studies on the impact of a few organic pesticides on certain fish enzymes.
  • Trasande, L., Massey, R. I., DiGangi, J., Geiser, K., Olanipekun, A. I., Gallagher, L. 2011. How developing nations can protect children from hazardous chemical exposures while sustaining economic growth. Health Affairs, 30(12): 2400-2409.
  • Valavanidis, A., Vlahogianni, T., Dassenakis, M., Scoullos, M. 2006. Molecular biomarkers of oxidative stress in aquatic organisms in relation to toxic environmental pollutants. Ecotoxicology and Environmental Safety, 64(2): 178-189.
  • Van der Oost, R., Beyer, J., Vermeulen, N. P. 2003. Fish bioaccumulation and biomarkers in environmental risk assessment: a review. Environmental Toxicology and Pharmacology, 13(2): 57-149.

Klorpirifosa Maruz Kalan Capoeta Umbla' nın Beyin Dokusunda Antioksidan Yanıtı

Yıl 2024, Cilt: 11 Sayı: 4, 1149 - 1153, 12.10.2024
https://doi.org/10.30910/turkjans.1546985

Öz

Klorpirifosun su ekosistemleri üzerindeki toksik etkileri üzerine yapılan bu çalışmada, Capoeta umbla türü balıkları model organizma olarak kullanılmıştır. Balıklara farklı konsantrasyonlarda (55-110 µg/L) ve sürede (24 ve 96 saat) klorpirifos uygulanarak, beyin dokusunda lipid peroksidasyonunun bir göstergesi olan malondialdehit (MDA) seviyesi ve antioksidan savunma sisteminin önemli enzimlerinden olan katalaz (CAT) ve glutatyon redüktaz (GR) aktiviteleri belirlenmiştir. Elde edilen sonuçlar, klorpirifosun balıklarda oksidatif stresi tetikleyerek hücre zarlarında lipid peroksidasyonunu artırdığını ve antioksidan savunma sistemini baskıladığını göstermiştir. Bu durum, klorpirifosun su ekosistemlerindeki canlılar üzerindeki olumsuz etkilerini ve çevresel riskini vurgulamaktadır.

Kaynakça

  • Ahmad, I., Hamid, T., Fatima, M., Chand, H. S., Jain, S. K., Athar, M., Raisuddin, S. 2000. Induction of hepatic antioxidants in freshwater catfish (Channa punctatus Bloch) is a biomarker of paper mill effluent exposure. Biochimica et Biophysica Acta (BBA)-General Subjects, 1523(1): 37-48.
  • Almeida, M., Fanini, F., Davino, S., Aznar, A., Koch, O., Barros, S. d. M. 1997. Pro-and anti-oxidant parameters in rat liver after short term exposure to hexachlorobenzene. Human & experimental toxicology, 16(5): 257-261.
  • Alves, S. R., Severino, P. c. C., Ibbotson, D. P., da Silva, A. Z., Lopes, F. R., Sáenz, L. A., Bainy, A. C. 2002. Effects of furadan in the brown mussel Perna perna and in the mangrove oyster Crassostrea rhizophorae. Marine Environmental Research, 54(3-5): 241-245.
  • Avci, A., Kaçmaz, M., Durak, İ. 2005. Peroxidation in muscle and liver tissues from fish in a contaminated river due to a petroleum refinery industry. Ecotoxicology and Environmental Safety, 60(1): 101-105.
  • Begum, G., Vijayaraghan, S. 1996. Alterations in protein metabolism of muscle tissue in the fish Clarias batrachus (Linn) by commercial grade dimethoate.
  • Beutler, E. 1984. A manual of biochemical methods. Red cell metabolism: 77-78.
  • Dar, O. I., Aslam, R., Pan, D., Sharma, S., Andotra, M., Kaur, A., Jia, A.-Q., Faggio, C. 2022. Source, bioaccumulation, degradability and toxicity of triclosan in aquatic environments: A review. Environmental Technology & Innovation, 25: 102122.
  • Hai, D. Q., Varga, S. I., Matkovics, B. 1997. Organophosphate effects on antioxidant system of carp (Cyprinus carpio) and catfish (Ictalurus nebulosus). Comparative Biochemistry and Physiology - C Pharmacology Toxicology and Endocrinology, 117(1): 83-88.
  • Hatami, M., Banaee, M., Haghi, B. N. 2019. Sub-lethal toxicity of chlorpyrifos alone and in combination with polyethylene glycol to common carp (Cyprinus carpio). Chemosphere, 219: 981-988.
  • Jin, Y., Chen, R., Liu, W., Fu, Z. 2010. Effect of endocrine disrupting chemicals on the transcription of genes related to the innate immune system in the early developmental stage of zebrafish (Danio rerio). Fish & Shellfish Immunology, 28(5-6): 854-861.
  • Jin, Y., Zhang, X., Shu, L., Chen, L., Sun, L., Qian, H., Liu, W., Fu, Z. 2010. Oxidative stress response and gene expression with atrazine exposure in adult female zebrafish (Danio rerio). Chemosphere, 78(7): 846-852.
  • Kavitha, P., Rao, J. V. 2007. Oxidative stress and locomotor behaviour response as biomarkers for assessing recovery status of mosquito fish, Gambusia affinis after lethal effect of an organophosphate pesticide, monocrotophos. Pesticide biochemistry and physiology, 87(2): 182-188.
  • Kelly, K., Havrilla, C. M., Brady, T. C., Abramo, K. H., Levin, E. D. 1998. Oxidative stress in toxicology: established mammalian and emerging piscine model systems. Environmental health perspectives, 106(7): 375-384.
  • Kirici, M. 2021. Toxicological Effects of Metal Ions and Some Pesticides on Carbonic Anhydrase Activity Purified from Bighead Carp (Hypophthalmichthys Nobilis) Gill Tissue. Carpathian Journal of Earth and Environmental Sciences, 16(1): 59-65.
  • Kirici, M., Atamanalp, M., Kirici, M., Beydemir, S. 2017. In vitro effects of some metal ions on glutathione reductase in the gills and liver of Capoeta trutta. Regulatory Mechanisms in Biosystems, 8(1): 66-70.
  • Kırıcı, M., Atamanalp, M., Kırıcı, M., Beydemir, Ş. 2020. Purification of glucose 6-phosphate dehydrogenase from Capoeta umbla gill and liver tissues and inhibition effects of some metal ions on enzyme activity. Marine Science and Technology Bulletin, 9(2): 92-101.
  • Kirici, M., Demir, Y., Beydemir, S., Atamanalp, M. 2016. The Effect of Al(3+) and Hg(2+) on Glucose 6-Phosphate Dehydrogenase from Capoeta Umbla Kidney. Applied Ecology and Environmental Research, 14(2): 253-264.
  • Kırıcı, M., Kırıcı, M., Atamanalp, M. 2017. In vitro Inhibition Effects of Some Metal Ions on Glutathione Reductase Purified from Capoeta trutta Kidney. Aquaculture Studies, 17: 385-394.
  • Kırıcı, M., Kırıcı, M., Atamanalp, M., Beydemir, Ş. 2021. Purification of glutathione reductase from some tissues of Capoeta umbla and the inhibitory effects of some metal ions on enzyme activity. Marine Science and Technology Bulletin, 10(2): 193-200.
  • Kirici, M., Kirici, M., Beydemir, S., Atamanalp, M. 2016. Purification of Carbonic Anhydrase from Capoeta umbla (Heckel, 1843) Gills and Toxicological Effects of Some Metals on Enzyme Activity. Turkish Journal of Fisheries and Aquatic Sciences, 16(1): 169-175.
  • Kirici, M., Kirici, M., Beydemir, S., Bulbul, M. 2017. Purification of Glucose 6-Phosphate Dehydrogenase from Gilthead Sea Bream (Sparus Aurata) Gill and Liver Tissues and Inhibition Effects of Some Metal Ions on Enzyme Activity. Fresenius Environmental Bulletin, 26(12): 7074-7082.
  • Kirici, M., Nedzvetsky, V. S., Agca, C. A., Gasso, V. Y. 2019. Sublethal doses of copper sulphate initiate deregulation of glial cytoskeleton, NF-kappa B and PARP expression in Capoeta umbla brain tissue. Regulatory Mechanisms in Biosystems, 10(1): 103-110.
  • Li, F., Ji, L., Luo, Y., Oh, K. 2007. Hydroxyl radical generation and oxidative stress in Carassius auratus liver as affected by 2, 4, 6-trichlorophenol. Chemosphere, 67(1): 13-19.
  • Liu, Y., Wang, J., Wei, Y., Zhang, H., Xu, M., Dai, J. 2008. Induction of time-dependent oxidative stress and related transcriptional effects of perfluorododecanoic acid in zebrafish liver. Aquatic Toxicology, 89(4): 242-250.
  • Lowry, O. H., Rosebrough, N. J., Farr, A. L., Randall, R. J. 1951. Protein measurement with the Folin phenol reagent. Journal of Biological Chemistry, 193(1): 265-275.
  • Lu, J., Wu, L., Newman, J., Faber, B., Gan, J. 2006. Degradation of pesticides in nursery recycling pond waters. Journal of agricultural and food chemistry, 54(7): 2658-2663.
  • Monteiro, P., Reis-Henriques, M., Coimbra, J. 2000. Plasma steroid levels in female flounder (Platichthys flesus) after chronic dietary exposure to single polycyclic aromatic hydrocarbons. Marine Environmental Research, 49(5): 453-467.
  • Ohkawa, H., Ohishi, N., Yagi, K. 1979. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Analytical Biochemistry, 95(2): 351-358.
  • Oruc, E. O., Sevgiler, Y., Uner, N. 2004. Tissue-specific oxidative stress responses in fish exposed to 2, 4-D and azinphosmethyl. Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology, 137(1): 43-51.
  • Oruç, E. Ö. 2010. Oxidative stress, steroid hormone concentrations and acetylcholinesterase activity in Oreochromis niloticus exposed to chlorpyrifos. Pesticide biochemistry and physiology, 96(3): 160-166.
  • Saha, S., Chukwuka, A. V., Mukherjee, D., Patnaik, L., Nayak, S., Dhara, K., Saha, N. C., Faggio, C. 2021. Chronic effects of Diazinon® exposures using integrated biomarker responses in freshwater walking catfish, Clarias batrachus. Applied Sciences, 11(22): 10902.
  • Sayeed, I., Parvez, S., Pandey, S., Bin-Hafeez, B., Haque, R., Raisuddin, S. 2003. Oxidative stress biomarkers of exposure to deltamethrin in freshwater fish, Channa punctatus Bloch. Ecotoxicology and Environmental Safety, 56(2): 295-301.
  • Sharma, S., Dar, O. I., Singh, K., Kaur, A., Faggio, C. 2021. Triclosan elicited biochemical and transcriptomic alterations in Labeo rohita larvae. Environmental Toxicology and Pharmacology, 88: 103748.
  • Thomas, P., Murthy, T. 1976. Studies on the impact of a few organic pesticides on certain fish enzymes.
  • Trasande, L., Massey, R. I., DiGangi, J., Geiser, K., Olanipekun, A. I., Gallagher, L. 2011. How developing nations can protect children from hazardous chemical exposures while sustaining economic growth. Health Affairs, 30(12): 2400-2409.
  • Valavanidis, A., Vlahogianni, T., Dassenakis, M., Scoullos, M. 2006. Molecular biomarkers of oxidative stress in aquatic organisms in relation to toxic environmental pollutants. Ecotoxicology and Environmental Safety, 64(2): 178-189.
  • Van der Oost, R., Beyer, J., Vermeulen, N. P. 2003. Fish bioaccumulation and biomarkers in environmental risk assessment: a review. Environmental Toxicology and Pharmacology, 13(2): 57-149.
Toplam 37 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Konular Balık Biyolojisi
Bölüm Araştırma Makalesi
Yazarlar

Mehmet Reşit Taysı 0000-0002-1072-4059

Erken Görünüm Tarihi 12 Ekim 2024
Yayımlanma Tarihi 12 Ekim 2024
Gönderilme Tarihi 10 Eylül 2024
Kabul Tarihi 26 Eylül 2024
Yayımlandığı Sayı Yıl 2024 Cilt: 11 Sayı: 4

Kaynak Göster

APA Taysı, M. R. (2024). Klorpirifosa Maruz Kalan Capoeta Umbla’ nın Beyin Dokusunda Antioksidan Yanıtı. Türk Tarım Ve Doğa Bilimleri Dergisi, 11(4), 1149-1153. https://doi.org/10.30910/turkjans.1546985